106259-86-3Relevant academic research and scientific papers
Parasiticidal pyrazoles
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, (2008/06/13)
Compounds of formula (I) or pharmaceutically, veterinarily or agriculturally acceptable salts thereof, or pharmaceutically, veterinarily or agriculturally acceptable solvates of either entity, wherein R1 is 2,4,6-trisubstituted phenyl or 3,5-disubstituted pyridin-2-yl; R3 is C1 -C4 alkyl optionally substituted with hydroxy or with one or more halo; cyano, C1 to C5 alkanoyl or phenyl; R5 is hydrogen, C1 to C4 alkyl, amino or halo; R2 and R4 are each independently selected from hydrogen, C1 to C4 alkyl, fluoro, chloro and bromo or, together with the carbon atom to which they are attached, form a C3 to C6 cycloalkyl group; R6 and R8 are each independently selected from hydrogen, C1 to C4 alkyl, fluoro, chloro and bromo; or, when R2 and R4 do not form part of a cycloalkyl group, R2 and R6, together with the carbon atoms to which they are attached, may form a C5 to C7 cycloalkyl group; and R7 is hydrogen, C1 to C4 alkyl optionally substituted with one or more halo, or C1 to C4 alkoxy; are parasiticidal agents.
Synthesis of a novel series of imidazo[4,5-c]pyrazole derivatives and their evaluation as herbicidal agents
Vicentini, Chiara B.,Manfrini, Maurizio,Mazzanti, Manuela,Scatturin, Angelo,Romagnoli, Carlo,Mares, Donatella
, p. 337 - 342 (2007/10/03)
Ever changing problems in agricultural weed control require periodic introduction of new herbicides. Imidazo[4,5-c]pyrazoles, which were considered of interest as potential herbicides, were synthesized and examined for the pre-emergence, post-emergence, and post-transplant control of weeds in rice against broadleaf and grass weed species. The data obtained suggest that some imidazo[4,5-c]pyrazoles have potential herbicidal activity against a wide range of weeds, with 5-methyl, 5-thiomethyl, and 5-unsubstituted derivatives being the most effective. No herbicidal activity was observed in the 5-methylsulfonylimidazo[4,5-c]pyrazole and imidazo[4,5-c]pyrazolone series.
Derivatives of N-phenylpyrazoles
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, (2008/06/13)
N-Phenylpyrazole derivatives of the formula: STR1 wherein R1 represents cyano, nitro, halogen, acetyl or formyl; R2 represents R5 SO2, R5 SO or R5 S in which R5 is optionally halogen substituted alkyl, alkenyl or alkynyl; R3 represents a hydrogen atom or a group NR6 R7 wherein R6 and R7 each represent hydrogen, alkyl, alkenylalkyl, alkynylalkyl, formyl, optionally halogen substituted alkanoyl, optionally halogen substituted alkoxycarbonyl, or alkoxymethyleneamino, halogen, or R6 and R7 together form a cyclic imide and R4 represents a substituted phenyl group possess arthropodicidal, plant nematocidal, anthelmintic and anti-protozoal properties; their preparation, compositions containing them and their use are described.
Pest-combating agents based on pyrazole derivatives
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, (2008/06/13)
A 5-aminopyrazole of the formula (I) STR1 in which R2 represents CF3 or CCL2 F, R3 represents hydrogen or CH3 and n represents the number 0 or 1. The 5-aminopyrazole of formula (I) is effective in com
1-aryl-4-alkylthiopyrazol-5-amine derivatives, composition containing them, and method of using them to combat insects, arachnids, and nematodes
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, (2008/06/13)
A method of combating insects, sense animals and nematodes comprising applying to insects, arachnids and nematodes and/or their environment an effective amount of at least one 5-aminopyrazole of the formula (I) STR1 in which R1 represents hydro
Pesticidal 1-arylpyrazoles, compositions and use
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, (2008/06/13)
Insecticidally active 1-aryl-pyrazoles of the formula STR1 in which R1 represents hydrogen, alkyl or haloalkyl, R2 represents alkyl, alkenyl, alkinyl, cycloalkyl, haloalkyl, haloalkenyl, alkoxyalkyl, alkylthioalkyl, alkylsulphinylalk
